Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the eye (HP:0000478)help
Parent Node:
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Abnormal eye morphology (HP:0012372)help
..Starting node
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obsolete Abnormal globe morphology (HP:0012374)help
Term ID: 12374
Name: obsolete Abnormal globe morphology
Synonym:
Definition:
Comments:
Reference: HP:0012374
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of the uvea (HP:0000553) help
................... HP:0000525 Abnormality iris morphology
................... HP:0000554 Uveitis
................... HP:0000610 Abnormal choroid morphology
................... HP:0008055 Aplasia/Hypoplasia affecting the uvea
................... HP:0012776 Abnormality of the ciliary body
........expandAbnormal sclera morphology (HP:0000591) help
................... HP:0000592 Blue sclerae
................... HP:0001140 Epibulbar dermoid
................... HP:0007832 Pigmentation of the sclera
................... HP:0025339 Superficial episcleral hyperemia
................... HP:0025340 Deep episcleral hyperemia
................... HP:0025513 Scleral rupture
................... HP:0025534 Ocular melanocytosis
................... HP:0030823 Scleral thickening
................... HP:0030854 Scleral staphyloma
................... HP:0100011 Scleral schwannoma
................... HP:0100532 Scleritis
................... HP:0100534 Episcleritis
........expandPhthisis bulbi (HP:0000667) help
........expandAbnormal anterior segment morphology (HP:0004328) help
................... HP:0000481 Abnormal cornea morphology
................... HP:0000517 Abnormality of the lens
................... HP:0000525 Abnormality iris morphology
................... HP:0000593 Abnormal anterior chamber morphology
................... HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
................... HP:0012627 Pseudoexfoliation
................... HP:0012628 Abnormal suspensory ligament of lens morphology
........expandAbnormal morphology of the posterior segment of the globe (HP:0004329) help
................... HP:0001098 Abnormal fundus morphology
................... HP:0004327 Abnormal vitreous humor morphology
................... HP:0030601 Abnormal posterior segment imaging
........expandAbnormality of the vasculature of the eye (HP:0008047) help
................... HP:0007905 Abnormal iris vasculature
................... HP:0008046 Abnormality of the retinal vasculature
................... HP:0008054 Abnormal vasculature of the conjunctiva morphology
................... HP:0025337 Red eye
........expandAplasia/Hypoplasia affecting the eye (HP:0008056) help
................... HP:0000528 Anophthalmia
................... HP:0000568 Microphthalmia
................... HP:0008055 Aplasia/Hypoplasia affecting the uvea
................... HP:0008057 Aplasia/Hypoplasia affecting the fundus
................... HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
........expandSpontaneous rupture of the globe (HP:0010727) help
........expandAbnormality of globe location (HP:0100886) help
................... HP:0000316 Hypertelorism
................... HP:0000490 Deeply set eye
................... HP:0000520 Proptosis
................... HP:0000601 Hypotelorism
................... HP:0009914 Cyclopia
................... HP:0030867 Vertical orbital dystopia
........expandAbnormality of globe size (HP:0100887) help
................... HP:0000528 Anophthalmia
................... HP:0000568 Microphthalmia
................... HP:0001090 Abnormally large globe

 Sister Nodes: 
..expandNeoplasm of the eye (HP:0100012) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012374HP:0012374obsolete Abnormal globe morphology0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.